Method and apparatus for purifying and packaging uranium hexachloride



Nov. 13, 1951 c. H. PRESCOTT, JR

METHOD AND APPARATUS FOR PURIFYING AND PACKAGING URANIUM HEXACHLORIDE 5 Sheets-Sheet 1 Filed Sept. 2, 1944 INVENTOR. CHARLES H. Pmsscorr JR.

ATTORNEY.

3 Sheets-Sheet 2 Iii 22 C. H. PRESCOTT, JR METHOD AND APPARATUS FOR PURIFYING AND PACKAGING URANIUM HEXACHLORIDE Nov. 13, 1951 Filed Sept. 2, 1944 ATTORNEY METHOD AND APPARATUS FOR PURIFYING AND PACKAGING URANIUM HEXACHLORIDE Nov. 13, 1951 c H. PRESCOTT, JR 2,574,842

Fild Sept. 2, '1944 5 Sheets-Sheet 3 INVENTOR. CHARLES H. PRESCOTT 1/3.

Maw

A TORN Patented Nov. 13, 1951 METHOD AND APPARATUS FOR PURIFYING AND PACKAGING URANIUM HEXACHLO- RIDE Charles H. Prescott, Jr., Berkeley, Calif., assignor to the United States of America asrepresented by the United States Atomic Energy Commission Application September 2, 1944, Serial No. 552,556

3 Claims. (01. ea-14.5)

x This invention relates to processes of an apparatus for packaging, and especially to closing, in the absence of air, receptacles containing material that is rapidly decomposed or otherwise affected deleteriously when exposed to atmospheric conditions. More particularly, it appertains to the purification of, and the filling of vaporizing vessels with, a, uranium chloride and to the hermetic sealing, under vacuum, of the charged vessels.

There is a present need for large quantities of the uranium isotope having mass number 235. Uranium as obtained from natural sources comprises the aforementioned isotope mixed with two others having the mass numbers 234 and 238, in the ratio U l: :U :120: :U :16,700. A11 apparatus capable of effecting a separation of desired components from a mixture of these isotopes, is called a calutron. Such a calutron essentially comprises means for vaporizing a quantity of material containing an element (for example, uranium) which is to be enriched with a selected one of its plurality of isotopes; means for subjecting the vapor to ionization, whereby at least a portion of the Vapor is ionized causing ions of the several isotopes of the element to be produced; electrical means for segregating the ions from the un-ionized vapor and for accelerating the segregated ions to relatively high velocities; electromagnetic means for deflecting the ions along curved paths, the radii of curvature of the paths of the ions being proportional to the square roots of'the masses of the ions, whereby the ions are concentrated in accordance with their masses; and means for de-ionizing and collecting the ions of the selected isotopes thus concentrated, thereby to produce a deposit of the element enriched with the selected isotope.

- The device for supplying the vapor of a material, such as a uranium compound, that is to be treated in a calutron ordinarily comprises a heater with a tubular chamber in which is set a vaporizing vessel, commonly called a charge bottle, containing a charge of a uranium compound that volatilizes readily upon heating. Uranium hexachloride, which can be satisfactorily sublimed at about 100 C. under mm. mercury vacuum, has been found to be especially suitable for charging these devices. Likewise,

uranium tetrachloride although normally less volatile is suitable for this purpose. However, both uranium tetrachloride and uranium hexachloride arehighly hygroscopic compounds and decompose readily when exposed-to atmospheric conditions. a i

For example, when uranium hexachloride is loaded into a charge bottle under ordinary atmospheric conditions, the uranium hexachloride particles usually become covered with a coating, probably uranyl chloride (UO2C12). This coating impedes volatilization, thereby necessitating higher vaporizing temperatures which, in turn, induce decomposition of the charge to relatively involatile uranium compounds.

The invention has for an object the vacuum packaging of a. hygroscopic material such as hy-. groscopic uranium compounds. Other objects are to fill and seal calutron charge bottles under vacuum, to provide a satisfactory process and ap-- paratus for purifying and packaging uranium compounds under vacuum, and to seal hermetically vacuum containers charged with uranium compounds. Further objects .are the production of a package comprising a wide-mouthed metal bottle having a closure soldered thereto and containing uranium hexachloride under vacuum; the prevention of deterioration during preparation, purification, packaging, storage, transport, etc, of uranium hexachloride; and the sublimation and storage of uranium hexachloride in vacuums as high as 10? mm. Hg absolute. Additional objects are to isolate a uranium chloride in a' vacuum, tosublime a uranium chloride in which are suitable for use in this process are uranium hexachloride, uranium tetrachloride, and the like.

An apparatus suitable for purifying and packaging the hygroscopic uranium compound comprises a subliming chamber, a condensing chamber joined there'to, a storage receptacle and a conduit connecting the condensing chamber and storage receptacle, means for maintaining a vacuum in the apparatus, means forheating the subliming chamber whe'reby' the uranium compound is sublimed into and "condensed in the condensing chamber, means for moving the sublimed and condensed uranium compound into the conduit and the storage receptacle, and means for hermetically sealing the charged storage receptacle.

I-Iow the foregoing objects and related ends are accomplished will be apparent from the following description including the principle, the organization and divers embodiments of the invention, and the best mode contemplated for carrying out the same. Parts are given by weight throughout the description; and the description is amplified by the accompanying drawings, in which:

Fig. 1 is a fragmentary side elevational view of combined charge purifying and charge bottle filling and sealing apparatus embodying the features of the invention.

Fig. 2 is a fragmentary plan view of the end of the material moving device employed in the coni densing .end of the apparatus of Fig. 1.

Fig. 3 is a side elevational view of the device of Fig. 2.

Fig. 4 is an end elevational view of the device of Fig. 2.

Fig. 5 is a fragmentary plan view of the end of the material moving device employed in the feeder end of the apparatus of Fig. 1.

Fig. 6 is a side elevational view of the device of Fig. 5.

Fig. 7 is an end elevational view of the device of Fig. 5.

Figs. 8 and 9 are enlarged fragmentary side elevational views, partly in section, of the apparatus of Fig. 1, illustrating the closing hood and the storage bottle secured thereto, certain of the parts being shown in different manipulated positions.

Fig. 10 is an enlarged perspective view of the parts of the frame which is employed to secure the storage bottle to the closing hood, certain of the parts being illustrated in exploded position.

Fig. 11 is a greatly enlarged fragmentary sectional view of the upper portion of the charge bottle and the bottle cap, illustrating the sealing arrangement therebetween.

Fig. 12 is a side elevational view, partly in section, of a modified form of charge bottle sealing apparatus embodying the features of the invention.

Fig. 13 is a fragmentary side elevational view of a pivot joint embodied in the McLeod gauge forming a part of the apparatus of Fig. 12.

Referring now to Figs. 1 to 7, inclusive, of the drawings, there is illustrated a purifying and packaging apparatus constructed largely of glass and comprising a hopper I0 in which the material to be processed is placed before the purification operation is started. A hopper having a capacity of about one liter is suitable. This hopper has a conduit ll through which it is filled with raw material, a tubular extension I 2 designed to receive a conventional high vacuum type of seal, such as described in vol. 112 (1941) pages 41-43, Review of Scientific Instruments and generally known as a Wilson seal, such seal 19 having a vacuum testing connection tube [9a, and a duct I3 for connection to a vacuum-producing apparatus (not shown). A removable plug it} fitting tightly in the conduit H closes this part of the apparatus against the ingress of air.

Raw material is released from the hopper as desired by means of a feeding device comprising a stainless steel disk-like gate l5. This gate, comprising two slightly warped semicircular metal sheets, is carried on a rod l6 that extends through the Wilson seal l9 and is operated by a handwheel H. A cylindrical rod made of onequarter inch stainless or ordinary carbon steel stock is suitable. Rotation of the handwheel l1 produces rotation of the gate [5 which thereupon functions like a feed screw to-release material from the hopper in conventional manner.

The hopper I0 is connected to a subliming container or kiln 20 by means of a duct l4, through which the raw material is delivered by gravity when released by the gate I5. Ordinarily, the container 20 is a 2.25-inch diameter Pyrex glass cylinder about 50 inches long. The container 20 has two downwardly extending delivery ducts or tubes 2| and 22. The sublimed and purified material is transmitted to a charge bottle or other receptacle I31 through the tube 22, and unsublimed material is moved through the tube 2| to a receptacle 40 connected thereto at 29. The container 20 also has tubular extensions 23, 24 and 25 constituting portals for the devices that manipulate the materials being processed, and two ducts 26 and 21, located exteriorly of the path of the material as it is processed, for connections to apparatus capable of producing a vacuum of at least 10* mm. of mercury. A gastight joint 28 is provided to facilitate assembling and cleaning of the apparatus. I

Near its center the horizontally disposed container 26 has a subliming zone surrounded by a furnace 30. This furnace consists of two semicylindrical electrical resistance heaters 3i and 32, capable of raising the batch of material being processed to its volatilization temperature; The temperature commonly reached in subliming uranium hexachloride in this apparatus is about to C., or even as high as 210 C. The heaters have individual electrical connections 33 and 34 for a source of heating current. The heater sections are constructed to provide space for a thermocouple Well 35. The thermocouple therein (not shown) is connected by conductors 36 and 31 to an indicating and/or recording instrument 38, such as a potentiometer or voltmeter, which may be suitably calibrated to indicate and/or record directly in terms of the temperature prevailing within the subliming zone.

For moving material inside the vessel 20 at the feeder end, an implement comprising a rod 4| carrying a chisel 44 and a hoe 43 is provided. To insure adequate rigidity, this rod should be about one-quarter inch in diameter. The rod 4| extends through a conventional Wilson seal 42 in the tubular extension 23, and carries on its external end a handwheel 45 by which the implement is manipulated. The chisel 44 and hoe 43 are ordinarily made ofstainless steel. The hoe is preferably in the form of an approximately 120 helical sector, tilted at an angle of about 22.5 to a plane normal to the axis of the rod, so that by rotating the rod M the hoe can be screwed into the mass of granular material in the chamber without pushing the entire mass of material forward, thus breaking up lumps or aggregates of the material.

For testing the gastightness of the connection around the rod 4|, the Wilson seal 42 has, as is usual with these devices, a lateral tube 46 for connection to vacuum-producing apparatus.

At the delivery end of the container 20, in the tubular extension 24, there is a similar material manipulating arrangement comprising a rod carrying a chisel 54 and a scraper blade 53, a sur-' face of which is substantially normal to the axis of the rod. As clearly shown in Figs. 1 to 4, the chisel portion 54 comprises one chisel surface adapted to contact more or less closely the wall surface of chamber 29 in order to scrape sublimate therefrom, and a second chisel surface extending ahead of, and substantially at right angles to, the first chisel surface, thereby functioning to split portions of the sublimate away from the main bulk thereof before the first chisel surface can develop a wedge action upon the main mass of sublimate when the tool is driven in' a direction generally parallel to the wall surface. It will also be noted that the second chisel surface slopes with respect to the axis of the rod,:

the usual (12) deflection for the rod 5|, as is customary in the conventional Wilson seal, such as seal 42. This improved seal is described in U. S. Patent to Starr 2,442,622. The greater range of movement is obtained by an arrangement including a swivel joint. This joint, located between the case carrying the diaphragms (not shown) and the plug fitting into the extension 24, is covered by a conventional flexible thin metal bellows 51. This bellows is soldered to the aforementioned parts to better maintain the vacuum inside.

The tubular extension 25 on top of the container 20 carries a conventional Wilson seal 52, incorporating a vacuum tseting connection tube 06. A rod 6|, which extends through the Wilson seal 62, has a pointed and/or notched end 64 and carries adjacent thereto a small hook 53* by an integral, laterally projecting flange 51..

This arrangement forms a continuous passage, whereby material falling through the duct 22 is conducted into the interior of the charge bottle, thereby avoiding an accumulation of charge materialin fine particle or dust form on the top of the bottle adjacent the closure, which accumulation of material would interfere with sealing the closure.

The hood 1| comprises a flange I5 conforming to the top of the bottle I3| and a laterally extending tubular portion I4 that forms a housing for a rod 8| that is supported Within a ,conventional Wilson seal 90. This rod, preferably of one-quarter inch round stock, is manipulated by a handwheel 85 and carries on its inner end; @9 1 retur during h qt le fil i r tion, supports a cap I for the charge bottle I 3| in a position within the lateral extension I4 where the cap cannot interfere with the descent of material into the charge bottle (Fig. 1 position). The hook 63 on the rod 6| supports the telescopic spout I3 above the mouth of the charge bottle I3I while the bottle is being capped (Fig. 8.

position).

The conventional Wilson seal that closes the tubular extension 14 comprises a plug part 99 having a. seat upon which a rubber diaphragm 9| is supported. A circular spacer 92 engages the diaphragm 9| and, in turn, is engaged by a second rubber diaphragm 93. This assembly is maintained in position by a washer 94 and a screw plug 95. A vent 91 in the annular piece 92 connects' the space between the rubber diaphragms 9| and 93 to a tube 96. This tube is employed as a.vacuum connection for testing the adequacy of the seal made between the rod 8| and the two diaphragms 9| and 93. By evacuating the tube 95,

it is possible to determine before the processing of material is started whether or not a gastight seal between the rod 8| and the plug 99 is formed by either or both of the diaphragms 9| and 93.

The charge bottle I 3| is cylindrical in shape and has a circular mouth I32 in the top. Surrounding the mouth is a groove I33 designed to receive the depending skirt or flange I42 of the cap MI and a groove I39 for packing purposes.

Ordinarily, the mouth I32 and grooves I33 and I39 arelocated concentrically in the top of the bottle. Preferably, the charge bottles are made of stainless steel, for example, 18-8 (l8-Cr, 8-Ni U. S. S. #316) stock, but other nonmagnetic met-;

als not readily attacked by the vapors of uranium halides may be used if desired.

In order to assist in providing a soldered gascomprise a noble metal such as silver, gold, etc.)

is shown, out of proportion for clarity, at I35 in r Fig. 11.

The charge bottle |3| is secured to the hood 1| while being filled and closed by a cage-like frame I00. This frame comprises a split ring that grips the bottle |3I and a split collar that extends over the flange I5 on the hood. The split ring is made up of two parts I 0| and I02 and the split collar consists of two semicircular parts I05 and I06. The part I02 is drilled at Ill and H8 and the part IOI is drilled and tapped at I I9 and I20 to receive screws I03 and I04 by means of which the split ring is caused to clamp the bottle. Similarly, the part I06 is drilled at I21 and I28 and the part I05 is drilled and tapped at I29 and I30 to receive screws I01 and I08 which hold the collar parts together on the flange I5. The aforementioned parts of the frame I 00 are usually made of brass. I

The frame I00 also comprises a series of bolts III, H2, H3, H4, H5 and H6 and cooperating nuts,-such as I24, I25 and I26, which connect the ring and collar. By tightening these nuts the charge bottle I3 I, being securely held by the split ring, is forced toward the hood II. This action applies pressure to an annular gasket I38, preferably made of rubber, positioned in the groove I39,

and produces a vacuum-tight seal between the bottle I3I and the hood 'II. A fiat ring I09, also preferably made of rubber, serves as a cushion between thesplitcollar of frame I00 and fran-L- gible flange .'|5..onv the hood II.. The gasket I38 of a built sufllcient. to preventxactual=contactof the bottle topand the flange 15.

The cap I4:I used for closing the mouth 13.2 of the charge bottle I31 comprises auflatxdisk-like main body or cover part and a depending skirt I42. This can intended for magnetic removal, is formed of magnetic material and. is provided with a peripheral, depending skirt I42 of variable height so that when cap I4] isrsoldered into -.position. it will be magnetically asymmetrical with reference to the axis of :the container. In order to assist in providing a soldered gastight; joint.

between the cap 141 and'the bottle I31. thei'skirt I42 is coated or plated with asmeta'l easily wet by the lowmeltingalloy, Woods:metal,:previously mentioned. The platin -is shown, outof proportion for clarity, at I45. in Fig. 1-1. Preferably, the layerof wetting metal r35 coating. the interior of the groove I83 and the layer of metal I45 coating theexterior of the skirt I42 are plated thereon and-comprise ametal such asa noble metal ('e. g., silver, gold, platinum, iridium, or osmium). A hermetic seal between the cap MI and the bottle I31 isobtained more easily if, before the-start of the sealing operation, a layer of the 'Woodsmetal solder I46 is wiped onto the layer I45ca-rried'by the skirt I42 and a ring of the Woods metal solder I36 is melted onto the layer [35 carried within the groove I33. After the bottle .I=3I :is filled and the sealing operation is carried out, the masses of solder I36 and I46 readily fuse-together, formin a gas-tight seal. between the cap I4 I and-thezbottle =I3l.

The top of the cap I 4'I removably supports an electric heater I5I, the heater ,I5JI being secured in place by :an arrangement including a screw I41 engaging a centrally disposed threaded hole provided in the cap .I4-I. This arrangement .accommodates heating of the cap iI-4I .in order to melt the previously mentioned bodies of solder H6 and I46. element, one terminal of which is connected or grounded to the cap I M and the other-terminal of which is connected to a terminal post I52 in the form of a loop or eyelet. The circuit for the heater .I-5I may be completed, as illustrateddiagrammatically in Fig. 9, by setting the notched end 64 of the rod 65 against the loop 152 and by connecting the rod GI and the bottle J31 to a suitable current source I55, the circuit arrangement utilizing two contactors I53 and I 54 and two connecting conductors I 56 andv I.5'I -as welbas asuitable switch (not shown). The heater I5I may be readily removed from the cap MIv by r emoving the screw I41 after the bottle .I.3 ,I has been sealed and disconnected from .the associated hood II.

Considering now the mode of operation of the apparatus shown in Figs. 1 to 11, inclusive, the

hopper It is filled with a mass, of raw or crude hygroscopic material I6I (such as uranium Zhexachloride) in subdivided form through the con.- duit .II, and the plug 18 .is fitted into the .end of the conduit I I in gastight relation. ,A quantity of glass .or other relatively inert material 1.60 in the form of powder or small beads :isplaced in the container 20- in a position from which it-can be later advanced toward the sublimingzone for a purpose to be noted hereinafter; apreviously preparedcap I'M is suspended upon thei-hook 83 carried by the rod 81 in the tubular extension 14;; a previouslyprepared charge bottle I 3;I visrseclmzd and sealed to the hood "by the. frame LIllllpthe spout 'I3;being adjusted :in themouth 132' ;of :the charge bottle, Ifilr; the receptacle is :secured to The heater $51 includesaresistance 8. the tube-2t; and. the. joints 2,8 and 29 :are closed. Preferably, the joints 28 and 29, as well as the connections between the conduit H and the plug I'8iare sealed in a. gastight manner with ordinary sealing wax. Similarly, the connection between the tubular extension I2 and the Wilson seal I9, theconnection between the tubular extension 23 and the Wilson seal 4.2, the connection between the-tubular extension 24 and the Wilson seal 52, the connection between the tubular extension 25 and the Wilson seal 62, and the connection between the tubular extension i4 and the Wilson seal 90. are also sealed with sealing wax. The vacuum-testing tubes Isa, 46, 5.6, 66 and 96, respectively associated with the Wilson seals I9, 42,, 52,, .62 and 9B are suitably connected to the Vflcuumrproducing apparatus and the Wilson seals mentioned. are tested in order to insure that the apparatus as a whole is gastight. The ducts I3,

, 26 and 21 are then connected to the vacuumproducing apparatus, whereby the container 20 and the connected parts are evacuated to a relatively-low pressure, such for example as 10- mm. Hg.

Abortion of the crude uranium hexachloride IBI is. introduced into the container 28 by suitably rotating or reciprocating the handwheel IT in order to control the gate I5, and is positioned in theheating zone within the furnace, as shown at I16 3,-by means of the hoe 43. Thereafter the subdivided glass or other inert material I60 is spread overthe adjacent or feed side of the pile of crude uranium hexachloride, as shown at IE4, thereby preventing or substantially preventing the flow of yapors toward the feed side of the apparatus; heat is then applied, causing volatilization of the uranium hexachloride, the vapor of which flows toward the cooler portion of the container 26 and condenses thereon, as shown at I65. Accordingly, ,it will be-noted that the portion of the container lying between the heater 30 and the duct 25, functions as an air-cooled condenser; it may be additionally noted that when and if desired, supplemental cooling structure, such as a surrounding coil through which is circulated a cooling medium such as water, may be provided at this point.

The condensate of uranium hexachloride usually begins to appear when the charge has reached a temperature of approximately C. However, temperatures somewhat in excess of 150 C., for example in the range of approximately 150 to 190 C., are preferred for the sublimation of this material atapractical rate. The sublimation of the UClc may be carried to substantial completion by raising the temperature. to about 210 'C. for a short time (up to about thirty minutes) at the end of a run at the lower temperature mentioned. The use of the higher temperature for extended periods is ordinarily not desired because uranium hexachloride begins to decompose, slightly at C., and at an appreciable rateabove C. in vacuo.

Thelayer of glass I64 serves to retard or prevent the flow of volatilized uranium compound in the opposite direction. When the vaporization of the charge has been completed, the glass and residual matter from the charge is raked back and into the receptacle 4,0 as shown at 165, exceptfcr a portion which preferably is retained in the tube 20 between ducts I4 and 2| to serve as a vapor blocking layer for the succeeding mass of crude material being processed. Another portion of the crude material I6I is then admitted to thetube 20 from the hopper I0 and is positioned in the-heating zone as-shown at I63, after which-itls'co'vered with a'layer I64 of subdivided glass and nonvaporized material from a previous run or runs, and another vaporization cycle is conducted. These cycles are repeated without breaking vacuum until the supply of crude uranium hexachloride lti has been exhausted.

The condensed uranium hexachloride I65 that collects on the cooler portions of the wall of the container 20 is chiseled away, preferably after each sublimation, with the chisel 54 and raked into the duct 22 with the hoe 53. The sublimate is deposited on the inside of the tube 20 in a zone ordinarily extending from about one-half inch to twelve inches from the edge of the hot zone,

with the thickest deposit usually occurring in the first three inches. The uranium hexachloride that sublimes below 170 C. condenses in this three-inch zone in a layer usually about %-inch thick. This deposit has a mechanical strength about equal to that of anthracite coal and must be chiseled off the wall. However, the adhesion between the deposit and the glass is somewhat weaker than its internal strength or cohesion, so that the deposit scales or breaks off in large pieces, particularly when the wall surface of the container 20 is clean. Pieces too large to pass through the duct 22 may be chopped into smaller pieces by means of the pointed rod 6!.

Although by this method all of the sublimed and purified uranium hexachloride may not be completely removed from the wall of the container 20, and although some slight amount of uranium hexachloride vapor may have seeped through the glass barrier I64 and deposited in solid form in the feed end of the tube 20, it is unnecessary to clean the tube after each run as dry air (which might remain in extremely small amount in the apparatus) causes no visible decomposition of the uranium hexachloride. It is therefore customary practice to clean the entire apparatus only after a number of runs.

A single run of the type described above usually requires a full working day and produces approximately one-half kilogram of highly purified uranium hexachloride, these figures being exemplary and based upon the particular apparatus chosen by way of illustrating the invention.

Care should be taken to avoid any jarring of the feed material during the subliming operation,

as this may cause flakes of this material to break loose and be blown into the condensation zone by the stream of uranium hexachloride vapor, and thus eventually contaminate the purified sublimed uranium hexachloride, Such contamination is not desirable since the presence of impurities may interfere with satisfactory operation of the calutron.

Instead of treating an impure uranium hexachloride to obtain the desired highly purified uranium hexachloride product as described above, uranium pentachloride may be employed as the starting material for the production of uranium hexachloride by the reaction mechanism disclosed and claimed in the copending patent of Francis A. Jenkins, No. 2,572,156, October 23, 1951; i. e., by the disproportionation of uranium pentachloride into uranium hexachloride and uranium tetrachloride under the influence of heat. When uranium pentachloride is used as the starting material I 6 I, it is heated in the subliming zone to a temperature ranging from about to about C., but preferably toward the upper end of this range. Temperatures as high as 250 C. may be employed for short periods, so as not to cause undue decomposition of the produced uranium hexachloride. At this temperature, andu'nder high vacuum, the uranium pentachloride is decomposed into uranium tetrachloride and uranium hexachloride, the latter passing out of the heated zone in the form of vapor which is condensed in the cooler portion of the container 20 from which it is removed and loaded into the charge bottle 13 I, as more fully described above. A residue, mainly uranium tetrachloride,

of over 50% of the original material is left in the sublimation zone. As this residue accumulates in the sublimation zone during and as aresult of the disproportionation of successive charges of uranium pentachloride and the attendant vaporization of uranium hexachloride produced thereby, 'the undesired accumulation of residue is raked into the duct 2| and collected in thereceiver 40 at desired intervals for suitable salvage operations, preferably however retaining each time sufficient or the residue in the container 20 to serve as a blocking layerfor the succeeding charge of uranium pentachloride that is positioned in the subliming zone.

Uranium tetrachloride of more or less impure form may also be used as the starting material I 6| where it is desired to prepare and/or package this compound in highly purified form for'subsequent treatment in a calutron or for any other purpose. In such purification and packaging, the apparatus functions in a manner'generally 'similar to that already described for the case of uranium heaxchloride,-except that a considerably higher temperature, such as 512 to 520 C. is preferably employed for subliming the uranium tetrachloride since the latter is considerably less volatile than the former. In general, a temperature of at least 500' C. is preferably employed. Condensation ofpurified uranium tetrachloride in the cooler portions of the tube 20 is'ordinarily first observed at a temperature of about' 365" to 380 C., under the pressure conditions already set forth. However, temperatures of from approximately 500 to 550 C. or higher are required for the sublimation of the material at a practical rate. When these higher temperatures are employed it is desirable to provide additional support for the tube 20 to prevent any sagging of the tube due to the higher temperatures necessary for the sublimation of uranium tetrachloride at a practical rate. 1

It will be understood that when a sufficient quantity of sublimate of highly purified uranium hexachloride (or of highly purified uranium tetrachloride, when the starting material IBI comprises more or less impure uranium tetrachlo ride as described'above) has been deposited on the-wallsof the container 20 as shown at I65, the deposit is'removed from the walls, broken into suflic ently small particle size to pass through duct 22, and scraped into the duct by suitable manipulation through the corresponding Wilson seals of rod 5| carrying scraper 53 and chisel 54 and rod 6| having the pointed end 64. In this manner sufficient purified sublimate is collected to fill charge bottle l3l to the desired level.- Where two or more sublimation cycles are'required to obtain the desired quantity of sublimate care is taken to maintain the vacuum in the system between successive cycles, as previously mentioned. r

Having collected the desired quantity of purified sublimate in the charge bottle I, the rod Si is manipulated so that, hook 63 lifts the tele scopic spout 13 from the filling position shown in Fig. 1 to the capping position shown in Fig. 8,,

15- the rod 81 with its hook as carryi the cover is manipulated to move the cover from its re- -tractedcfillingpositionshown in Fig. l to the position shown :in Fig..8, and the cover is thereupon placed in the capping position shown .in l9 with its skirt M2 disposed in groove -t33. (It will be understood that the groove I33 in the top of .thezcharge bottle 13.! and theskirt [42 of the .cap sliflil will have been prepared previously for the :soldering operation, in the manner described more fully above in connection with Fig. 11.) Rodt8l is then manipulat on so that its hook .83

Isupportsthe spout'13, thereby freeingrod 6| with -its:hook-t63 for another purpose, as shown in Fig. 9'. .As also shown in that figure, rod 6! is then :manipulated' so that its notched end 64 bears firmly uponeyeletzl 52 that forms a terminal post for-the 'heaterzel'ement-r511 attached to the cover M of" the charge bottle. Now upon completing theelectrical circuit including the heater element' I51, thelatter' isenerg zed and thereby supplies sufficient heat Ito-cap: IM to melt the entire mass of Woods metal filling-groove 33.. The circuit is then opened'and, after cooling, theWoods metal :forms a hermetic seal between the skirt 1'42 of' the cover 14! and: the topof the charge'bottle PM. The frame Hlllmay then be unfastenedand the charge bottle 131 with its hermetically sealed contents removed from the apparatus. Another cover 1 4.1 and charge bottle I3l' (previously prepared for the soldering operation) may then be placed inpositon in the apparatus, and the puritying and sealing operations resumed.

'Referringnow to Figs. l2 and"13.'there is shown amodifi'ed apparatus designed solely for the sealing under vacuum of charge bottles containing hygroscopic material that may be similar in nature to any one of the materials already described. In this modification the tube 222 corresponds to the tube 22 in the modification of Fig. 1- sofar as the location and the function of servin as a duct 'for evacuating air or other gas -from the hood 2' are concerned. However, it does not have the function of transmitting the charge to the charge bottle that is one of the purposes of the tube 22. The hood 211 is constructedsimilarly to the'hood H and has a tubular extension 214, closed by means ofa 'Wilson seal 2911 A correspond ng rod 281' having a hook 283 and a handwheel 285 at its opposite ends operates in the tubular extension and through the Wilson seal. A charge bottle 23! is positioned against the flange 215 on the hood and acap 24! carrying a heater 24'! is located in the-hood over the mouth of the bottle 23f. A suitable frame (not shown) is provided to clamp the charge bottle to the hood during operations, the frame being similar to frame l flil shown in- F'ig. 1'1 and therefore not requiring further discussion. Also, a suitable current source (not shown) is provided for the heater element 241-, the circuit for same being completed through the charge bottle 23!, rod 281 and hook 283, the latter thus functioningsimilarly to rod 6| as already described in connection with Fig. 9.

The air or other gas within the hood 21'! is, during the operation of this device, evacuated through the: vertical tube 222 into the horizontal tube 210. from whence itenters-a trap device for condensing moisture and the like, comprising a bulb: 2| labout-whichi'spositioned a container 2| 2 for liquid air or similar cooling medium 2L3. Noncondensable gases leave the bulb 211 through vertical .exit tube 214 and pass through horizontal tube M5 andmercury ,diiiusion pump. 2|.6 into horizontal tube 2, vertical tube 218,, and.

within. the apparatus. from time to time.

12 horizontal tube 21:9 to a vacuum pump. A drying tube (not shown) provided. with a powerful desiccant, such as phosphorus pentoXide, is preferably detail .in Fig. .13) for shiftingthelocationof the mercury contained therein. The arms of the joint are" shown at 226 and 221. Glass columns 228 and 22-9 .add strength and rigidity to the device, thereby increasing: its ruggedness.

Thev mercury difiusion pump is of a conven tional type comprising a vaporizing vessel or :b0i'161'52'3-9 "heated by an electric resistance coil 2-3liuand containing a poolof meroury2'32'. Mer- .cury vapor produced in the boiler leaves the boiler through tube 233 and, after having its direction of flow reversed'fbythe-cap 23 5 supp0rted-on gl'ass (10111111111243, flows concurrently with the gas being evacuated from hood 211 in the condenser tube 235. The curtain of mercury vaporfibwingv past the annular opening between the cap 23 3 and the bulb in which itis situated promotes the removal of residual gas from the hood to be evacuated, in the Well-known manner characteristic of diffusion pumps. The condenser tube 235 is surrounded by a jacket 2'33 defining a space for theci'rculation of a cooling liquid such aswater. The cooling liquid enters through inlet 2-31 and leaves through outlet'23 8. The mercury condensed in the condenser tube 235' flows "therefrom through inclined tube 239' and collects in trap 2 46. When the condensed body of mercury 24! collects to a sufiicient height in the trap, it overflows through tube 242 back into the boiler 23!) where it combines with the main body of mercury for reevaporation to continue the cycle of pump op eration.

It will be understood that after a charge bot tle 23'! containing a charge of uranium chloride that is to be hermetically sealed within has been secured in place against the flange 215 and the desired degree of vacuum (of the order of l0- mm, of Hg absolute) placed upon the system, the sealing operation is carried out in a manner that will be perfectly apparent from a consideration of .Fig. 112 "taken with the previous description of the sealing operation as applied to charge bottle I3 I, and which for brevity need not be repeated.

For the sake of brevity, the vacuum-producing apparatus that is required. for the apparatus illustrated in Fig. 1 has not been shown in detail and it will be understood that it may be generally similar .in nature to that already described inconnection with Fig. 12. However, due to the much greater size of the apparatus of Fig. l, .the accessory apparatus preferably comprises-two liquid .air traps and .One mercury difiusion pump. In addition, two drying tubes provided with magnesium perchlorate and phosphorus pentoxide are. employed. to dry the stream. of air when. the apparatus is let .down. to. atmospheric. pressure.

The .extra. vacuum connecting line. 21. greatly improves the operation. of the. apparatus of Fig. 1,. It facilitates bringing the system under vacuum, particularly on first pumping down, because gases.

are removed directly from the discharge end of the system withouthaving to pass through the dam of packed powdered raw material (charge) to the vacuum-connecting line 26. Similar remarks apply to the vacuum-connecting line I3 which may be connected to the same vacuumproducing'apparatus as are lines 26 and 21. Producing a high vacuum in the system shown in Fig. 1 would be a very slow operation if a large volume of gases had to be evacuated through the tube 26 alone. In addition, any gas accidentally introduced during operation, for example by leakage at a Wilson seal, passes out of the device without passing over the heated charge.

When processing corrosive materials such as are described herein, it is desirable-particularly in view of the relatively elevated temperatures employed-to use specially selected materials of construction for the selected apparatus. Because of its heat resistance, Pyrex glass is the preferred material for constructing the principal parts of the apparatus. The rods l6, 4!, 5|, GI and BI, the hoes 43 and 53, the hooks 63 and 83 and the charge bottle l3! are preferably made of stainless steel stock, such as 18-8 (Cr-18, Ni-8 U. S. S. #316), in order to resist corrosion by chlorinecontaining materials inside the apparatus. The chisels or spikes 44 and 54 are made of tool steel. The preferred material for making the cap I4! is soft iron but any other material that is sumciently magnetic to be lifted from the bottle mouth by the magnetic field of a calutron and which has low magnetic retentivity is also suitable for this purpose. The iron commonly used is not easily wet by molten Woods metal (the material ordinarily used for soldering the cap to the charge bottle) so it is desirable, as explained above, that the skirt I42 on the cap l4l be coated or tinned with a metal that is readily wet by such an alloy. The Woods metal referred to above is a very low-melting material, usually the quaternary alloy 50 Bi, 25 Pb, 12.5 Sn and 12.5 Cd. This substance melts at 65.5. C. A silver solder comprising 63 Ag, 30 Cu and 7.5 Zn is especially suitable for tinning the skirt on the cap.

As illustrated above, the subliming container 2|] is about 2% inches in diameter and 50 inches long, having a heater providing a hot zone for sublimation that is about 10 inches long. It will be understood, of course, that these dimensions are given merely by way of illustration of one particular embodiment of the apparatus, and that they may be varied over a wide range, if so desired. The subliming operation should be carried out in a vacuum of 10- mm. of mercury or better.

Many of the advantages of the previously described apparatus and process will be apparent from the description and drawings. Particular attention may, however, be advantageously directed to certain features. By this invention a process has been provided whereby a highly hygroscopic uranium compound may be purified and/or packaged in a container that is adapted for use in a calutron, without exposing the compound to atmospheric conditions. In this manner the deterioration and decomposition of the compound is prevented during storage, transfer, etc. An apparatus has also been disclosed which is suitable not only for the purification and packaging of hygroscopic uranium compounds under vacuum, but "also for hermetically'sealing the vacuum containers. Obviously the disclosed process and apparatus may be used for handling of other hygroscopic materials where superior conditions of protection are .desired.

Probably many apparently widely different embodiments of this invention may be made without departing from the principle, breadth and spirit thereof and it is to be understood, therefore, that this invention is not limited to the specific embodiments thereof except as encompassed in the following claims.

What is claimed is:

1. The process of preparing and packaging uranium hexachloride comprising heating uranium pentachloride at a temperature below about 250 C. whereby uranium hexachloride is formed and exists as a vapor, condensing the vapor, thus obtained the hexachloride as a sublimate deposited in situ as a solid in the condensing zone, thereafter removing said solid deposit by splitting the same and separately charging the brokenapart sublimate into a container, and hermetically sealing the container, all while maintaining the uranium hexachloride under vacuum.

2. An apparatus for purifying a relatively volatile normally solid material that condenses directly to the solid state from the vapor state comprising an elongated, horizontally disposed, tubular chamber having a heated, centrally disposed, subliming zone and a cooled condensing zone axially spaced from said subliming zone and exhaust ducts leading to means for producing a high vacuum in said chamber, the ducts being located adjacent the opposite end portions of said chamber and so disposed as to produce a vacuum condition in said condensing zone and in the zone lying on the opposite side of said subliming zone, respectively, whereby a vacuum may be produced in the apparatus without setting up a fluid current over the material being processed, a feed hopper for a solid raw material that is capable of producing vapor of the desired relatively volatile normally solid material under the conditions obtaming in the heated subliming zone, the feed hopper being disposed above said chamber and communicating with the latter on the side of the subliming zone opposite the condensing zone, and a rigid implement extending axially of said chamber and manually operable from the exterior of the chamber for packing solid raw material from the feed hopper in the subliming zone.

3. Apparatus as defined in claim 2 and including a discharge conduit. extending downwardly from the condensing zone of said chamber and terminating in an increased diameter hood adapted to sealingly engage the mouth of a storage container, an integral, tubular portion extending laterally from said hood, elongated rigid means disposed within said latter portion and movable longitudinally and rotatably from the exterior of said portion for transporting a container closure from said portion into container sealing position in said hood, and means controllable from the exterior of said hood for hermetically sealing the closure upon said storage container.

CHARLES H. PRESCOTT, JR.

(References on following page) REFERENCES CITED:

file of this patent:

UNITED STATES PATENTS Number Name Date Smith, Jan. 28, 1890 Vautour et a1 May 20., 1902 Rigby Dec. 29, 1908 Johnson Sept. 8, 1914 Pier Nov. 9, 1915 Wander June 29, 1920 Waite Sept. 30, 1924 Number 16 Name: Date Brown Dec. 1, 1925 Noble Sept. 13, 1932 Amati Oct. 7, 1941 Alexander May 26,1942 Wade Oct. 12, 1943 OTHER REFERENCES Moore, Preparation of Metallic Uranium, m Transactions of the American Electrochemical Society, volume 43, pages 317-328, (1923).

Friend, Textbook of Inorganic Chemistry, volume VII, part III, pages 294 and 295, (1926). 

1. THE PROCESS OF PREPARING AND PACKAGING URANIUM HEXACHLORIDE COMPRISING HEATING URANIUM PENTACHLORIDE AT A TEMPERATURE BELOW ABOUT 250* C. WHEREBY URANIUM HEXACHLORIDE IS FORMED AND EXISTS AS A VAPOR, CONDENSING THE VAPOR, THUS OBTAINED THE HEXACHLORIDE AS A SUBLIMATE DEPOSITED IN SITU AS A SOLID IN THE CONDENSING ZONE, THEREAFTER REMOVING SAID SOLID DEPOSIT BY SPLITTING THE SAME AND SEPARATELY CHARGING THE BROKEN APART SUBLIMATE INTO A CONTAINER, AND HERMETICALLY SEALING THE CONTAINER, ALL WHILE MAINTAINING THE URANIUM HEXACHLORIDE UNDER VACCUM. 